Allele Registry

Canonical Allele Identifier: PA2826270896

Gene: APP HGNC NCBI

ClinVar RCV:

RCV000019713

RCV001386879

RCV002272024

ClinVar Variation:

18087

HGVS (amino-acid)	Matching Registered Transcripts
NP_001191232.1:p.Glu600Gln	CA127790 NM_001204303.2:c.1798G>C